Condensation of the Triad System with Carbonyl Compounds. I. Condensation of Ethyl Itaconate with Ketones
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概要
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In the presence of sodium ethoxide, ethyl itaconate condensed with ketones (acetone and cyclohexanone) at the terminal carbon atoms of its triad system without any appreciable isomerisation and afforded novel compounds, α-methyl-γ,γ-disubstituted aconic acids (C) and α-alkylidenemethyl-γ,γ-disubstituted aconic acids (D).<BR>(<U>Remark: Graphics omitted.</U>)<BR>The chemical structures of C and D were determined by ultraviolet, infrared, NMR spectra etc.<BR>A reaction mechanism has been proposed (p. 1197).
- 社団法人 日本化学会の論文
著者
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Katsuta Chiaki
Department of Chemistry Tokyo University of Education
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Sugiyama Noboru
Department of Chemistry Tokyo University of Education
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Sugiyama Noboru
Department of Chemistry Faculty of Science Tokyo University of Education
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Katsuta C.
Department of Chemistry Tokyo University of Education
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